DIAGNOSTIC ULTRASOUND VERSADOPP 1000

DIAGNOSTIC ULTRASOUND VERSADOPP 1000 is an FDA 510(k)-cleared medical device (K904792) manufactured by Diagnostic Ultrasound Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 27, 1991. Regulation: 8.